يعرض 1 - 10 نتائج من 53 نتيجة بحث عن '"A. M. Mamedyarov"', وقت الاستعلام: 1.03s تنقيح النتائج
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    المساهمون: Not specified., Отсутствует.

    المصدر: Current Pediatrics; Том 22, № 4 (2023); 305-310 ; Вопросы современной педиатрии; Том 22, № 4 (2023); 305-310 ; 1682-5535 ; 1682-5527

    وصف الملف: application/pdf

    العلاقة: https://vsp.spr-journal.ru/jour/article/view/3267/1312Test; Hingorani M, Hanson I, van Heyningen V. Aniridia. Eur J Hum Genet. 2012;20(10):1011–1017. doi: https://doi.org/10.1038/ejhg.2012.100Test; Воскресенская А.А., Поздеева Н.А., Васильева Т.А. и др. Клинические особенности врожденной аниридии в детском возрасте // Российская педиатрическая офтальмология. — 2016. — Т. 11. — № 3. — С. 121–129. — doi: https://doi.org/10.18821/1993-1859-2016-11-3-121-129Test; Tibrewal S, Ratna R, Gour A, et al. Clinical and molecular aspects of congenital aniridia — A review of current concepts. Indian J Ophthalmol. 2022;70(7):2280–2292. doi: https://doi.org/10.4103/ijo.IJO_2255_21Test; Bamiou DE, Free SL, Sisodiya SM, et al. Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations. Arch Pediatr Adolesc Med. 2007;161(5):463–469. doi: https://doi.org/10.1001/archpedi.161.5.463Test; Hu P, Meng L, Ma D, et al. A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation. Mol Cytogenet. 2015;8(1):3. doi: https://doi.org/10.1186/s13039-015-0110-2Test; Hanish AE, Butman JA, Thomas F, et al. Pineal hypoplasia, reduced melatonin and sleep disturbance in patients with PAX6 haplo-insufficiency. J Sleep Res. 2016;25(1):16–22. doi: https://doi.org/10.1111/jsr.12345Test; Lee HJ, Colby KA. A review of the clinical and genetic aspects of aniridia. Semin Ophthalmol. 2013;28(5-6):306–312. doi: https://doi.org/10.3109/08820538.2013.825293Test; Касман-Келнер Б., Вейстенц А., Зейц Б. Медицинское сопровождение врожденной аниридии и аниридийного синдрома (РАХ6-синдрома) // Практическая медицина. — 2015. — № 1-2. — C. 34–61.; Васильева Т.А., Поздеева Н.А., Воскресенская А.А. и др. Генетические аспекты врожденной аниридии // Практическая медицина. — 2015. — № 2-1 — С. 26–33.; Васильева Т.А., Воскресенская А.А., Поздеева Н.А. и др. Характеристика гена РАХ6 и роль его мутаций в развитии наследственной патологии органа зрения // Генетика. — 2018. — Т. 54. — № 9. — С. 979–987. — doi: https://doi.org/10.1134/S0016675818090151Test; Wawrocka A, Krawczynski MR. The genetics of aniridia — simple things become complicated. J Appl Genet. 2018;59(2):151–159. doi: https://doi.org/10.1007/s13353-017-0426-1Test; Васильева Т.А., Воскресенская А.А., Хлебникова О.В. и др. Дифференциальная диагностика наследственных форм врожденной аниридии с позиций современной генетики // Вестник РАМН. — 2017. — Т. 72. — № 4. — С. 233–241. — doi: https://doi.org/10.15690/vramn834Test; Ansari M, Rainger J, Hanson IM, et al. Genetic Analysis of ‘PAX6-Negative’ Individuals with Aniridia or Gillespie Syndrome. PLoS One. 2016;11(4):e0153757. doi: https://doi.org/10.1371/journal.pone.0153757Test; Kim KC, Lee DK, Go HS, et al. Pax6-dependent cortical glutamatergic neuronal differentiation regulates autism-like behavior in prenatally valproic acid-exposed rat offspring. Mol Neurobiol. 2014;49(1):512–528. doi: https://doi.org/10.1007/s12035-013-8535-2Test; Эль-Ансари А. ГАМК, дефициты нейротрансмиттера глутамата при аутизме и их нейтрализация как новая гипотеза эффективной стратегии лечения // Аутизм и нарушения развития. — 2020. — Т. 18. — № 3. — C. 46–63. — doi: https://doi.org/10.17759/autdd.2020180306Test; Glaser T, Jepeal L, Edwards JG, et al. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nature Genet. 1994;7(4):463–471. doi: https://doi.org/10.1038/ng0894-463Test; Tyas DA, Pearson H, Rashbass P, Price DJ. Pax6 regulates cell adhesion during cortical development. Cereb Cortex. 2003;13(6): 612–619. doi: https://doi.org/10.1093/cercor/13.6.612Test; Schmidt-Sidor B, Szymańska K, Williamson K, et al. Malformations of the brain in two fetuses with a compound heterozygosity for two PAX6 mutations. Folia Neuropathol. 2009;47(4):372–382.; Fischbach BV, Trout KL, Lewis J, et al. WAGR syndrome: a clinical review of 54 cases. Pediatrics. 2005;116(4):984–988. doi: https://doi.org/10.1542/peds.2004-0467Test; Yogarajah M, Matarin M, Vollmar C, et al. M. PAX6, brain structure and function in human adults: advanced MRI in aniridia. Ann Clin Transl Neurol. 2016;3(5):314–330. doi: https://doi.org/10.1002/acn3.297Test; Käsmann-Kellner B, Berthold S. Kongenitale Aniridie oder PAX6-Syndrom. Ophthalmologe. 2014;111(12):1144. doi: https://doi.org/10.1007/s00347-014-3058-4Test; Malandrini A, Mari F, Palmeri S, et al. PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation. Clin Genet. 2001;60(2):151–154. doi:https://doi.org/10.1034/j.1399-0004.2001.600210.xTest; Катаргина Л.А., Мазанова Е.В., Тарасенков А.О. Клинико-функциональные особенности врожденной аниридии и сочетанной с ней патологии // Российская педиатрическая офтальмология. — 2015. — Т. 10. — № 3. — С. 21–23.; Landsend ECS, Lagali N, Utheim TP. Congenital aniridia — A comprehensive review of clinical features and therapeutic approaches. Surv Ophthalmol. 2021;66(6):1031–1050. doi: https://doi.org/10.1016/j.survophthal.2021.02.011Test; Robinson DO, Howarth RJ, Williamson KA, et al. Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia. Am J Med Genet A. 2008;146A(5):558–569. doi: https://doi.org/10.1002/ajmg.a.32209Test; Bobilev AM, Hudgens-Haney ME, Hamm JP, et al. Early and late auditory information processing show opposing deviations in aniridia. Brain Res. 2019;1720:146307. doi: https://doi.org/10.1016/j.brainres.2019.146307Test; Bamiou DE, Campbell NG, Musiek FE, et al. Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutation. Int J Audiol. 2007;46(4):196–202. doi: https://doi.org/10.1080/14992020601175952Test; Кельмансон И.А. Хронопатологические аспекты расстройств сна и когнитивных функций у детей с нарушениями зрения // Российский вестник перинатологии и педиатрии. — 2015. — Т. 60. — № 5. — С. 42–50.; Berntsson SG, Kristoffersson A, Daniilidou M, et al. Aniridia with PAX6 mutations and narcolepsy. J Sleep Res. 2020;29(6):e12982. doi: https://doi.org/10.1111/jsr.12982Test; Moosajee M, Hingorani M, Moore AT. PAX6-Related Aniridia. 2003 May 20 [Updated 2018 Oct 18]. In: GeneReviews® [Internet]. Adam MP, Everman DB, Mirzaa GM, et al., eds. Seattle (WA): University of Washington, Seattle; 1993–2022.; Guo R, Zhang X, Liu A, et al. Novel clinical presentation and PAX6 mutation in families with congenital aniridia. Front Med (Lausanne). 2022;9:1042588. doi: https://doi.org/10.3389/fmed.2022.1042588Test; Дамулин И.В., Тардов М.В. Клинико-патогенетические особенности мозжечковой атаксии // Трудный пациент. — 2020. — Т. 18. — № 10. — С. 17–23. — doi: https://doi.org/10.24411/2074-1995-2020-10067Test; Grant MK, Bobilev AM, Pierce JE, et al. Structural brain abnormalities in 12 persons with aniridia. F1000Res. 2017;6:255. doi: https://doi.org/10.12688/f1000research.11063.2Test; Solomon BD, Pineda-Alvarez DE, Balog JZ, et al. Compound heterozygosity for mutations in PAX6 in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia. Am J Med Genet. 2009;149A(11):2543–2546. doi: https://doi.org/10.1002/ajmg.a.33081Test; Ugalahi MO, Ibukun FA, Olusanya BA, Baiyeroju AM. Congenital aniridia: Clinical profile of children seen at the University College Hospital, Ibadan, South-West Nigeria. Ther Adv Ophthalmol. 2021;13:25158414211019513. doi: https://doi.org/10.1177/25158414211019513Test; Генинг Г.Н. Влияние врожденной аниридии на палитру психических состояний пациентов с аниридией и родителей детей с аниридией // Семья и дети в современном мире: сборник материалов конференции. — СПб.: Изд-во РГПУ им. А.И. Герцена; 2019. — Т. 5. — С. 135.; Nishizawa H, Motobayashi M, Akahane M, et al. Neuro-psychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder. Brain Dev. 2022;44(3):229–233. doi: https://doi.org/10.1016/j.braindev.2021.11.06Test; Han JC, Liu QR, Jones M, et al. Brain-Derived Neurotrophic Factor and Obesity in the WAGR Syndrome. N Engl J Med. 2008;359(9): 918–927. doi: https://doi.org/10.1056/NEJMoa0801119Test; Shinawi M, Sahoo T, Maranda B, et al. 11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity. Am J Med Genet A. 2011;155:1272–1280. doi: https://doi.org/10.1002/ajmg.a.33878Test; Yamamoto T, Togawa M, Shimada S, et al. Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4. Am J Med Genet A. 2014;164A(3):634–638. doi: https://doi.org/10.1002/ajmg.a.36325Test; Duffy KA, Trout KL, Gunckle JM, et al. Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management. Front Pediatr. 2021; 9:733018. doi: https://doi.org/0.3389/fped.2021.733018Test; https://vsp.spr-journal.ru/jour/article/view/3267Test

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    دورية أكاديمية

    المصدر: Current Pediatrics; Том 16, № 1 (2017); 39-48 ; Вопросы современной педиатрии; Том 16, № 1 (2017); 39-48 ; 1682-5535 ; 1682-5527

    وصف الملف: application/pdf

    العلاقة: https://vsp.spr-journal.ru/jour/article/view/1729/680Test; Koman LA, Smith BP, Shilt JS. Cerebral palsy. Lancet. 2004;363(9421):1619–1631. doi:10.1016/S0140-6736(04)16207-7.; Семенова К.А. Восстановительное лечение детей с перинатальным поражением нервной системы и детским церебральным параличом. — М.: Закон и порядок; 2007. — 616 с. [Semenova KA. Vosstanovitel’noe lechenie detei s perinatal’nym porazheniem nervnoi sistemy i detskim tserebral’nym paralichom. Moscow: Zakon i poryadok; 2007. 616 p. (In Russ).]; Bax M, Goldstein M, Rosenbaum P, et al. Proposed definition and classification of cerebral palsy, April 2005. Dev Med Child Neurol. 2005;47(8):571–576. doi:10.1017/s001216220 500112x.; SCPE. Prevalence and characteristics of children with cerebral palsy in Europe. Dev Med Child Neurol. 2002;44(9):633–640. doi:10.1111/j.1469-8749.2002.tb00848.x.; Wichers MJ, Odding E, Stam HJ, van Nieuwenhuizen O. Clinical presentation, associated disorders and aetiological moments in cerebral palsy: a Dutch population-based study. Disabil Rehabil. 2005;27(10):583–589. doi:10.1080/09638280400018445.; Leonard J, Graham HK. Treatment of motor disorders in cerebral palsy with botulinum neurotoxin. In: Jankovic J, editor. Botulinum toxin: Therapeutic clinical practice and science. Philadelphia:Saunders Elsevier; 2009. p. 172–191. doi:10.1016/b978-1-4160-4928-9.00014-7.; Heinen F, Desloovere K, Schroeder AS, et al. The updated European Consensus 2009 on the use of Botulinum toxin for children with cerebral palsy. Eur J Paediatr Neurol. 2010;14(1): 45–66. doi:10.1016/j.ejpn.2009.09.005.; Novak I, McIntyre S, Morgan C, et al. A systematic review of interventions for children with cerebral palsy: state of the evidence. Dev Med Child Neurol. 2013;55(10):885–910. doi:10.1111/dmcn.12246.; Hagglund G, Wagner P. Development of spasticity with age in a total population of children with cerebral palsy. BMC Musculoskelet Disord. 2008;9:150. doi:10.1186/1471-2474-9-150.; Hagglund G, Andersson S, Duppe H, et al. Prevention of dislocation of the hip in children with cerebral palsy. The first ten years of a population-based prevention programme. J Bone Joint Surg Br. 2005;87:95–101. doi:10.1302/0301-620X.87B1.15146.; Pascual-Pascual S, Pascual-Castroviejo I. Safety of botulinum toxin type A in children younger than 2 years. Eur J Paediatr Neurol. 2009;13(6):511–515. doi:10.1016/j.ejpn.2008.10.006.; Druschel C, Althuizes HC, Funk JF, Placzek R. Off label use of botulinum toxin in children under two years of age: а systematic review. Toxins (Basel). 2013;5(1):60–72. doi:10.3390/toxins5010060.; Tilton AH. Evidence-based review of safety and efficacy in cerebral palsy. Toxicon. 2015;107(Pt A):105–108. doi:10.1016/j.toxicon.2015.09.020.; Simpson LL. Identification of the major steps in botulinum toxin action. Annu Rev Pharmacol Toxicol. 2004;44:167–193. doi:10.1146/annurev.pharmtox.44.101802.121554.; Scott AB. Development of botulinum toxin therapy. Dermatol Clin. 2004;22(2):131–133. doi:10.1016/s0733-8635(03)00019-6.; Koman LA, Mooney JF, Smith B, et al. Management of cerebral palsy with botulinum-A toxin: preliminary investigation. J Pediatr Orthop. 1993;13(4):489–495. doi:10.1097/01241398-199307000-00013.; Pascual-Pascual SI, Herrera-Galante A, Poo P, et al. [Guidelines for the treatment of child spasticity using botulinum toxin. (In Spanish).] Rev Neurol. 2007;44(5):303–309.; Arner M, Himmelmann K, Ponten E, et al. [Upper extremity botulinum toxin treatment in cerebral palsy. Treatment guidelines the first step towards national cooperation. (In Swedish).] Lakartidningen. 2008;105(43):3009–3013.; National Collaborating Centre for Women’s and Children’s Health (UK). Spasticity in children and young people with non-progressive brain disorders: management of spasticity and co-existing motor disorders and their early musculoskeletal complications. London: RCOG Press; 2012. p. 293.; Delgado M, Hirtz D, Aisen M, et al. Practice parameter: pharmacologic treatment of spasticity in children and adolescents with cerebral palsy (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. 2010;74(4):336–343. doi:10.1212/WNL.0b013e3181cbcd2f.; Placzek R. [Botulinum toxin A in children with infantile cerebral palsy: indications and treatment concepts. (In German).] Orthopade. 2010;39(1):23–30. doi:10.1007/s00132-009-1534-3.; Corry IS, Cosgrove AP, Duffy CM, et al. Botulinum toxin A compared with stretching casts in the treatment of spastic equinus: a randomised prospective trial. J Pediatr Orthop. 1998;18(3): 304–11. doi:10.1097/01241398-199805000-00006.; Graham HK, Aoki KR, Autti-Ramo I, et al. Recommendations for the use of botulinum toxin type A in the management of cerebral palsy. Gait Posture. 2000;11(1):67–79. doi:10.1016/S0966-6362(99)00054-5.; Molenaers G, Fagard K, Van Campenhout A, Desloovere K. Botulinum toxin A treatment of the lower extremities in children with cerebral palsy. J Child Orthop. 2013;7(5):383–387. doi:10.1007/s11832-013-0511-x.; Rathinam C, Bateman A, Peirson J, Skinner J. Observational gait assessment tools in paediatrics — a systematic review. Gait Posture. 2014;40(2):279–285. doi:10.1016/j.gaitpost.2014.04.187.; Metaxiotis D, Siebel A, Doederlein L. Repeated botulinum toxin A injections in the treatment of spastic equinus foot. Clin Orthop Relat Res. 2002;(394):177–185. doi:10.1097/00003086-200201000-00021.; Goldberg MJ. Botulinum toxin type a improved ankle function in children with cerebral palsy and dynamic equinus foot deformity. J Bone Joint Surg Am. 2000;82(6):874. doi:10.2106/00004623-200006000-00016.; Love SC, Valentine JP, Blair EM, et al. The effect of botulinum toxin type a on the functional ability of the child with spastic hemiplegia a randomized controlled trial. Eur J Neurol. 2001;8 Suppl 5: 50–58. doi:10.1046/j.1468-1331.2001.00038.x.; Fehlings D, Rang M, Glazier J, Steele C. Botulinum toxin type a injections in the spastic upper extremity of children with hemiplegia: Child characteristics that predict a positive outcome. Eur J Neurol. 2001;8 Suppl 5:145–149. doi:10.1046/j.1468-1331.2001.00047.x.; Wissel J, Heinen F, Schenkel A, et al. Botulinum toxin A in the management of spastic gait disorders in children and young adults with cerebral palsy: a randomized, double-blind study of «highdose » versus «low-dose» treatment. Neuropediatrics. 1999;30(3): 120–124. doi:10.1055/s-2007-973475.; Fazzi E, Maraucci I, Torrielli S, et al. Factors predicting the efficacy of botulinum toxin-a treatment of the lower limb in children with cerebral palsy. J Child Neurol. 2005;20(8):661–666. doi:10.1177/08830738050200080501.; Gough M, Fairhurst C, Shortland AP. Botulinum toxin and cerebral palsy: time for reflection? Dev Med Child Neurol. 2005;47(10): 709–712. doi:10.1017/S0012162205001453.; Cosgrove AP, Corry IS, Graham HK. Botulinum toxin in the management of the lower limb in cerebral palsy. Dev Med Child Neurol. 1994;36(5):386–396. doi:10.1111/j.1469-8749.1994. tb11864.x.; Heinen F, Molenaers G, Fairhurst C, et al. European consensus table 2006 on botulinum toxin for children with cerebral palsy. Eur J Paediatr Neurol. 2006;10:215–225. doi:10.1016/j.ejpn.2006.08.006.; Molenaers G, Schorkhuber V, Fagard K, et al. Long-term use of botulinum toxin type A in children with cerebral palsy: treatment consistency. Eur J Paediatr Neurol. 2009;13(5):421–429. doi:10.1016/j.ejpn.2008.07.008.; Naumann M, Albanese A, Heinen F, et al. Safety and efficacy of botulinum toxin type A following long-term use. Eur J Neurol. 2006; 13 Suppl 4:35–40. doi:10.1111/j.1468-1331.2006.01652.x.; Willis AW, Crowner B, Brunstrom JE, et al. High dose botulinum toxin A for the treatment of lower extremity hypertonicity in children with cerebral palsy. Dev Med Child Neurol. 2007;49(11):818–822. doi:10.1111/j.1469-8749.2007.00818.x.; Crowner BE, Brunstrom JE, Racette BA. Iatrogenic botulism due to therapeutic botulinum toxin A injection in a pediatric patient. Clin Neuropharmacol. 2007;30(5):310–313. doi:10.1097/WNF.0b013e31804b1a0d.; Naidu K, Smith K, Sheedy M, et al. Systemic adverse events following botulinum toxin A therapy in children with cerebral palsy. Dev Med Child Neurol. 2010;52(2):139–144. doi:10.1111/j.1469-8749.2009.03583.x.; Клочкова О.А., Куренков А.Л., Намазова-Баранова Л.С., и др. Общее моторное развитие и формирование функции рук у пациентов со спастическими формами детского церебрального паралича на фоне ботулинотерапии и комплексной реабилитации // Вестник Российской академии наук. — 2013. — Т. 68. —№ 11 — С. 38–48. [Klochkova OA, Kurenkov AL, Namazova-Baranova LS, et al. Development of motor functions and manual abilities in pediatric patients with spastic cerebral palsy after botulinum toxin treatment and complex rehabilitation. Annals of the Russian academy of medical sciences. 2013;68(11):38–48. (In Russ).] doi:10.15690/vramn.v68i11.842 (In Russ).]; Куренков А.Л., Клочкова О.А. Ботулинотерапия детского церебрального паралича. В кн.: Азбука ботулинотерапии / Под ред. С.Л. Тимербаевой. — М.: Практическая медицина; 2014. — С. 148—171. [Kurenkov AL, Klochkova OA. Botulinoterapiya detskogo tserebral’nogo paralicha. In: Timerbaeva S.L., editor. Azbuka botulinoterapii. Moscow: Prakticheskaya meditsina; 2014. p. 148–171. (In Russ).]; Калинина Л.В., Сологубов Е.Г., Лузинович В.М., Дутикова Е.М. Ботокс в комплексном лечении детского церебрального паралича // Журнал невропатологии и психиатрии им. С.С. Корсакова. — 2000. — Т. 100. — № 12 — С. 60–63. [Kalinina LV, Sologubov EG, Luzinovich VM, Dutikova EM. Botoks v kompleksnom lechenii detsko go tserebral’nogo paralicha. Zh Nevrol Psikhiatr Im S S Korsakova. 2000;100(12):60–63. (In Russ).]; Калинина Л.В., Дутикова Е.М. Детский церебральный паралич. В кн.: Применение Ботокса (токсина ботулизма типа А) в клинической практике: руководство для врачей / Под ред. O.P. Орловой, H.H. Яхно. — М.: Каталог; 2001. — С. 86–107. [Kalinina LV, Dutikova EM. Detskii tserebral’nyi paralich. In: Orlova O.P., Yakhno N.N., editors. Primenenie Botoksa (toksina botulizma tipa A) v klinicheskoi praktike: rukovodstvo dlya vrachei. Moscow: Katalog; 2001. p. 86–107. (In Russ).]; Сальков В.Н., Лильин Е.Т., Степанченко О.В., и др. Ботокс при трицепс-синдроме у детей с детским церебральным параличом //Журнал неврологии и психиатрии им. С.С. Корсакова. — 2002. — Т. 102. — № 5 — С. 24–25. [Sal’kov VN, Lil’in ET, Stepanchenko OV, et al. Botoks pri tritseps-sindrome u detei s detskim tserebral’nym paralichom. Zh Nevrol Psikhiatr Im S S Korsakova. 2002;102(5): 24–25. (In Russ).]; Куренков А.Л., Батышева Т.Т., Никитин С.С., и др. Лечение спастичности у детей с церебральными параличами. Методические рекомендации № 15 Департамента здравоохранения города Москвы. — М.; 2011. — C. 3–5. [Kurenkov AL, Batysheva TT, Nikitin SS, et al. Lechenie spastichnosti u detei s tserebral’nymi paralichami. Metodicheskie rekomendatsii № 15 Departamenta zdravookhraneniya goroda Moskvy. Moscow; 2011. p. 3–5. (In Russ).]; Куренков А.Л., Батышева Т.Т., Виноградов А.В., Зюзяева Е.К. Спастичность при детском церебральном параличе: диагностика и стратегии лечения // Журнал неврологии и психиатрии им. С.С. 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  8. 8
    دورية أكاديمية

    المساهمون: 10.15690/vsp.v16i4.1780

    المصدر: Current Pediatrics; Том 16, № 4 (2017); 326-333 ; Вопросы современной педиатрии; Том 16, № 4 (2017); 326-333 ; 1682-5535 ; 1682-5527

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  9. 9
    دورية أكاديمية

    المصدر: Pediatric pharmacology; Том 13, № 3 (2016); 259-269 ; Педиатрическая фармакология; Том 13, № 3 (2016); 259-269 ; 2500-3089 ; 1727-5776

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